A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544891



Internal ID20918129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30921956..30924064hg38UCSC Ensembl
chr22:31317943..31320051hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382109
hg192109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073705
Samples
Known GenesMORC2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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